Canonical Allele Identifier: PA2826701163
Gene: ARHGAP30 HGNC NCBI

Linked Data

ClinVar Variation Id: 3128740
ClinVar RCV Id: RCV004422624
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274529.1:p.Cys765Ser
CA343320237
NM_001287600.2:c.2294G>C
CA343320239
NM_001287600.2:c.2293T>A